Immune responses to adenovirus and adeno-associated virus in humans

被引:567
作者
Chirmule, N
Propert, KJ
Magosin, SA
Qian, Y
Qian, R
Wilson, JM
机构
[1] Univ Penn, Inst Human Gene Therapy, Stellar Chance Labs 304, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Mol & Cellular Engn, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
[4] Univ Penn, Dept Biostat & Epidemiol, Philadelphia, PA 19104 USA
[5] Wistar Inst, Philadelphia, PA 19104 USA
关键词
adenovirus; AAV; neutralizing antibodies; lymphoproliferation; cytokines; humans;
D O I
10.1038/sj.gt.3300994
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vectors based on human adenovirus (Ad) and adenoassociated Virus (AAV) are being evaluated for human gene therapy. The response of the host to the vector, in terms of antigen-specific immunity, will play a substantial role in clinical outcome. We have surveyed cohorts of normal subjects and cystic fibrosis patients for pre-existing immunity to these viruses, caused by naturally acquired infections. A number of humoral and cellular assays to adenovirus serotype 5 (Ad5) and adeno-associated virus serotype 2 (AAV2) were performed from serum and peripheral blood mononuclear cells. Virtually all subjects had Ig to Ad5 although only 55% of these antibodies neutralized virus (NAB). Approximately two of three patients demonstrated CD4(+) T cells that proliferated to Ad antigens of which most were of the TH, subset, based on cytokine secretion. A substantially different pattern of immune responses was observed to AAV2. Although virtually all patients had Ig to AAV2, most of these antibodies were not neutralizing (32% NAB) and only 5% of patients had peripheral blood lymphocytes that proliferated in response to AAV2 antigens. These studies demonstrate marked heterogeneity in pre-existing immunity to Ad5 and AAV2 in human populations. The impact of these findings on outcome following gene therapy will require further study.
引用
收藏
页码:1574 / 1583
页数:10
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